WO2000001327A2 - Joint prosthesis, in particular finger joint prosthesis - Google Patents

Joint prosthesis, in particular finger joint prosthesis Download PDF

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Publication number
WO2000001327A2
WO2000001327A2 PCT/NL1999/000413 NL9900413W WO0001327A2 WO 2000001327 A2 WO2000001327 A2 WO 2000001327A2 NL 9900413 W NL9900413 W NL 9900413W WO 0001327 A2 WO0001327 A2 WO 0001327A2
Authority
WO
WIPO (PCT)
Prior art keywords
joint prosthesis
cylindrical
socket
joint
prosthesis according
Prior art date
Application number
PCT/NL1999/000413
Other languages
French (fr)
Other versions
WO2000001327A3 (en
Inventor
Paul Henricus Poeschmann
Cornelis Marinus Van Leeuwen
Original Assignee
Van Straten Beheer B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Van Straten Beheer B.V. filed Critical Van Straten Beheer B.V.
Priority to EP99931585A priority Critical patent/EP1094766B1/en
Priority to AT99931585T priority patent/ATE262862T1/en
Priority to JP2000557775A priority patent/JP2004525652A/en
Priority to AU48036/99A priority patent/AU4803699A/en
Priority to US09/720,983 priority patent/US6352560B1/en
Priority to DE69916064T priority patent/DE69916064T2/en
Publication of WO2000001327A2 publication Critical patent/WO2000001327A2/en
Publication of WO2000001327A3 publication Critical patent/WO2000001327A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/42Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes
    • A61F2/4241Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
    • A61F2002/30138Convex polygonal shapes
    • A61F2002/30153Convex polygonal shapes rectangular
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30574Special structural features of bone or joint prostheses not otherwise provided for with an integral complete or partial collar or flange
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30621Features concerning the anatomical functioning or articulation of the prosthetic joint
    • A61F2002/30624Hinged joint, e.g. with transverse axle restricting the movement
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30621Features concerning the anatomical functioning or articulation of the prosthetic joint
    • A61F2002/30624Hinged joint, e.g. with transverse axle restricting the movement
    • A61F2002/30632Hinged joint, e.g. with transverse axle restricting the movement with rotation-limiting stops, e.g. projections or recesses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2002/30934Special articulating surfaces
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/42Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes
    • A61F2/4241Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers
    • A61F2002/4243Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers for interphalangeal joints, i.e. IP joints
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/42Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes
    • A61F2/4241Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers
    • A61F2002/4251Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers for metacarpo-phalangeal joints, i.e. MCP or MP joints, e.g. knuckle joints
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2/4637Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for connecting or disconnecting two parts of a prosthesis
    • A61F2002/4641Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for connecting or disconnecting two parts of a prosthesis for disconnecting
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0002Two-dimensional shapes, e.g. cross-sections
    • A61F2230/0017Angular shapes
    • A61F2230/0019Angular shapes rectangular
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00029Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium

Definitions

  • Joint prosthesis in particular finger joint prosthesis
  • the present invention relates to a joint prosthesis comprising a first part with a cylindrical socket and a second part with a cylindrical head, the cylindrical head and socket being complementary to one another, in such a manner that together they are able to form a linear hinge which extends in the longitudinal direction of the head/socket.
  • a prosthesis of this nature is known, in the form of a finger joint prosthesis, from US-A-3, 991, 425.
  • a prosthesis of this nature, or at least a prosthesis which appears extremely similar, is also known under the name Djoa prosthesis.
  • the Djoa prosthesis comprises a cylindrical roll surface in which a slot is formed.
  • a hollow cylindrical socket runs over the cylindrical roll surface, with a projection which projects out of the socket fitting into the slot.
  • this projection is to prevent the socket from moving sideways, i.e. in the longitudinal direction of the linear hinge, with respect to the cylindrical roll surface, in order to ensure stability of the joint prosthesis in relation to loads which act in the longitudinal direction of the hinge.
  • a drawback of this design is that in the event of such loads a force is exerted on the underlying bones to which the joint is attached, via the slot with the projection situated therein. As a result, the stems may be dislodged from the underlying bone or may break off, which would lead to considerable damage to the underlying bone.
  • GB patent specification 1,530,301 has disclosed a finger prosthesis which differs from the joint prosthesis according to the present invention in particular by the fact that the socket parts are fixed to the head parts by means of a snap-action connection, i.e. the socket parts extend over more than 180°, as is clear from the figures. Owing to the snap-action connection, this prosthesis, in the implanted position, does not allow any movement of the prosthesis parts with respect to one another apart from the pivoting movement about the longitudinal axis of the head parts/socket parts. It is not possible for the prosthesis parts to move apart from one another and to pivot with respect to one another transversely to the hinge direction.
  • DE-Offenlegungsschrift 2,814,752 has disclosed a two-part joint prosthesis, in which the first part comprises a fork with a socket part inside.
  • the second part is provided with a head part which can be fixed to the socket part by means of a snap-action connection. Since the head part is of spherical or convex design, and the socket part is shaped accordingly, this joint prosthesis has two degrees of freedom. In addition to the main hinged movement, limited pivoting with respect to the main hinged movement is also possible.
  • the prosthesis disclosed by DE-2,814,752 cannot move apart in the implanted position.
  • the object of the present invention is to provide a joint prosthesis which, on the one hand, provides so-called medial/lateral stability, so that it is impossible for the moving parts to move in the longitudinal direction of the hinge with respect to one another, and, on the other hand, allows transverse forces, acting in the longitudinal direction of the hinge, on the bones which are connected by the joint without this inevitably leading to excessive load on the connection between the joint parts and the respective bones to which they are attached.
  • this object is achieved by means of a special design of the joint prosthesis, and in particular by the fact that: the cylindrical socket extends over at most 180° in the circumferential direction, the cylindrical head is provided with a radial thickened section which extends in the circumferential direction, and the cylindrical socket is provided with a radial recess which extends in the circumferential direction and in which the radial thickened section can be accommodated, preferably with the cylindrical head bearing inside the cylindrical socket .
  • the cylindrical head can be removed from the cylindrical socket by pulling it out in a direction which is parallel to or lies between the tangents at the free ends of the extent of the cylindrical socket.
  • this essentially means that this bone is pulled away from the joint in its longitudinal direction.
  • this also means that when, in this position, a transverse force which is directed in the longitudinal direction of the linear hinge acts on the said bone, this bone can undergo a pivoting movement, during which the cylindrical head comes out of the socket at one end of the linear hinge and is pressed against the socket at the other end of the linear hinge.
  • a self- aligning effect of this nature can be achieved in a wide variety of ways by suitable shaping of circumferential sides, which extend in particular in the circumferential direction, of the radial thickened section and/or the radial recess.
  • the self-aligning effect can be achieved, inter alia, by providing the circumferential sides of the radial thickened section with bevels and/or rounded portions, optionally in combination with bevels and/or rounded portions on the circumferential sides of the radial recess.
  • the circumferential sides, which extend in the circumferential direction, of the radial thickened section and/or of the radial recess comprise an active circumferential side face which includes an angle of approximately 1° to approximately 10° with a radially oriented transverse plane. These side faces therefore do not extend at right angles to the axis of rotation of the linear hinge, but rather at a relatively small angle with respect to a radial transverse plane which is perpendicular to the said hinge axis.
  • the cylindrical head is arranged on the end of at least one support arm which extends radially with respect to the cylindrical head, if one or both longitudinal edge(s) of the cylindrical socket are provided, in the area of the at least one support arm, with a cutout in which the cross section of the support arm can be completely or partially accommodated.
  • the freedom of rotation of the linear hinge in one or both direction (s) of rotation is greater than the associated freedom of rotation (medical: flexural freedom) of the natural joint which the joint prosthesis is intended to replace.
  • the extent to which this freedom of rotation of the joint prosthesis is greater than that of the natural joint will preferably be approximately 5° to approximately 20°, such as for example, and more preferably, approximately 15°.
  • the first part and the second part are each a metal part, for example are each a single-piece metal part. It is thus possible to produce joint prostheses which, in relative terms, are extremely small and yet strong, such as for example finger joint prostheses.
  • the metal parts are in this case preferably made from a chromium-cobalt alloy, as is known per se from the prior art for prostheses and joint prostheses.
  • first part and the second part, or at least the contact surfaces of the cylindrical head and cylindrical socket are coated with a suitable coating material.
  • the first and second parts, or at least their external surfaces are made from or coated with a material which is compatible with the human, or if appropriate animal, body, i.e. in particular a material which is compatible with the human, or if appropriate animal, body without entering into chemical reactions therewith, or at least without entering into any adverse and/or undesirable chemical reactions therewith.
  • the cylindrical socket extends over at least 160°, preferably over at least 170°, in the circumferential direction.
  • MCP metacarpophalangeal
  • PIP proximal interphalangeal
  • Figure 1 shows a perspective view of a joint prosthesis according to the invention in the so-called extended state
  • Figure 2 shows a perspective view of the embodiment shown in Figure 1, but with the parts of the joint prosthesis taken apart;
  • Figure 3 shows a side view, partially in section, of a joint prosthesis in accordance with the embodiment shown in Figures 1 and 2 which has been pivoted into a limit position;
  • Figure 4 shows a rear view, from the direction of arrow IV, of one part of the joint prosthesis according to the invention
  • Figure 5 shows an extremely diagrammatic sketch of the cylindrical socket, on the basis of which the directions in which the cylindrical head can be removed from the cylindrical socket are indicated;
  • Figure 6 shows a diagrammatic view of the bones and joints of which a finger is composed.
  • Figure 1 shows a diagrammatic, perspective view of a so-called PIP prosthesis, the view being from above onto the underside, in the implanted position, of the joint prosthesis, i.e. the side which lies on the inside of the hand in the implanted position.
  • joint part 1 is the proximal joint part, which lies on the carpal (metacarpal) side of the joint, i.e. that side of the joint which is directed towards the hand.
  • the joint part 2 is the distal joint part which lies on that side of the joint which is directed towards the fingertips.
  • Both joint parts comprise a stem which is known per se, or at least is nothing special, and by means of which the joint prosthesis can be attached in a respective phalangeal bone of the hand using techniques which are known per se. It is entirely within the scope of the invention for these stems 3 and 4 also to be of different design, for example as a multiple stem for mutually parallel pins or with a different shape from that which is illustrated in the figures .
  • the proximal part 1 is provided with a head 5, in which a cylindrical socket 6 is formed.
  • the centre of the cylindrical socket 6 is provided with a recess 7 which extends in the circumferential direction of the cylindrical socket 6, divides the cylindrical socket 6 in two and is likewise of cylindrical form. This recess 7 thus forms, as it were, a deeper, additional cylindrical socket surface between the two parts of the cylindrical socket 6.
  • the cylindrical socket 6, or at least its purely central part, extends over 175 to 180°, and will preferably extend over approximately 180°.
  • the distal part 2 of the joint prosthesis is provided with a cylindrical head 8 which extends essentially over 360° and is provided in its centre with a radial thickened section 9 which extends over virtually the entire circumference of the cylindrical head 8. Those parts of the cylindrical head 8 which lie next to the central thickened section extend over 360°.
  • the radial thickened section 9 extends over less than 360°, since it is interrupted by a support arm 10, via which the cylindrical head 8, 9 is connected to the stem 4.
  • An oval flange 11 is formed between the support arm 10 and the stem 4, providing support on the underlying bone and preventing the distal part 2 of the joint prosthesis from being pressed too deep into the associated bone.
  • the cylindrical head 8 and cylindrical socket 6 are shaped so as to complement one another, in such a manner that the cylindrical head 8 can be accommodated in the cylindrical socket 6 and can execute a hinged movement about the common, describing cylinder axis.
  • the width of the thickened section 9, as seen in the direction of the hinge axis 12, i.e. in the longitudinal direction of the head/socket, is essentially equal to the width of the recess 7 in the cylindrical socket 6, as seen in the same direction.
  • the thickened section 9 is dimensioned in such a manner that it can be accommodated entirely inside the recess 7, in which position there is no need for the cylindrical circumferential surfaces, which run parallel to the longitudinal direction, of the recess and the thickened section as such to be in contact with one another. It will be clear that the thickened section 9 thus prevents the distal joint prosthesis part 2 from being displaced in the longitudinal direction of the linear hinge with respect to the proximal joint prosthesis part 1, since the essentially radial circumferential side faces 14 of the thickened section 9 and the essentially radial circumferential side faces 13 of the recess will be in contact, or virtually in contact, with one another.
  • the distal joint prosthesis part 2 may execute a pivoting movement, in the direction of arrow 15, with respect to the proximal joint prosthesis part 1, in which case one end of the cylindrical head 8 will come out of the cylindrical socket 6 and the other, opposite end of the cylindrical head 8 will be pressed into the cylindrical socket 6.
  • a force which acts on the distal phalangeal bone of the hand in the transverse direction, indicated by arrow F, can result in tilting or pivoting, in the direction of arrow 15, of the distal joint prosthesis part 2 with respect to the proximal joint prosthesis part 1, without this leading to a load being imposed on the connection between the stems 3 and 4 and the proximal phalangeal bone of the hand or distal bone of the hand, since the pivoting indicated by arrow 15 and caused by the transverse force F is then absorbed by the natural or artificial joint ligaments.
  • the thickened section and/or recess are preferably both shaped so as to be self- aligning. According to the invention, this can be achieved, inter alia, by bevelling the circumferential sides 14 of the thickened section 9 at 15 and by bevelling the circumferential sides 13 of the recess 7 at 16.
  • the self-aligning action can be improved further by providing the circumferential sides 14 circumferential side faces which slope slightly towards one another in the radially outward direction, for example each slope at an angle of from 1 to 10° with respect to a transverse plane which is perpendicular to the hinge axis 12.
  • the circumferential sides of the recess can be provided with circumferential sides faces which slope towards one another in the same direction, also preferably at an angle of from 1 to 10° with respect to a transverse plane which is perpendicular to the hinge axis 12.
  • the cylindrical socket 6 is provided with a cutout 17 on its underside, which is shown as the top side in Figures 1 and as the underside in Figure 3.
  • the dimensions of the cutout 17 are such that it is able to accommodate the support arm 10, so that the freedom of rotation of the distal joint prosthesis part 2 with respect to that of the proximal joint prosthesis part 1 is made greater than the extent in the circumferential direction of the cylindrical socket would inherently allow.
  • distal joint prosthesis part 2 it is possible for the distal joint prosthesis part 2 to be over-extended, by an angle ⁇ of 25°, in the upwards direction with respect to the extended position illustrated in Figure 3 by the axis 18 (in the medical field, this is also known by the term hyperextension) , and also that the distal joint prosthesis part 2 can rotate downwards, in the anticlockwise direction, over an angle ⁇ of 125° in the downwards direction (also known in the medical field by the term flection) .
  • Figure 5 provides a very diagrammatic side view of a cylindrical socket which extends over 150° in the circumferential direction.
  • 61 and 62 are in this case the tangents on the opposite ends of the cylindrical extent of the socket 60. These tangents 61 and 62, with their intersection point, together determine a range ⁇ of tension directions T via which the cylindrical head can be pulled out of the cylindrical socket.
  • the arrow T in this case runs within the tangent lines 61 and 62 and intersects the intersection of these tangents.
  • Figure 6 provides a highly diagrammatic illustration of the bones of a finger and the joints of a finger.
  • 71 denotes the carpal bones, which for their part comprise a number of small bones and joints
  • 72 denotes the proximal phalange
  • 73 denotes the middle phalange
  • 74 denotes the distal phalange.
  • the joint 75 as indicated by the letters MCP, is the so-called metacarpophalangeal joint
  • 76 is the so-called PIP (proximal interphalangeal) joint
  • 77 is the so- called DIP (distal interphalangeal) joint.
  • the natural freedom of movement of an MCP is, in the upward overextended direction, generally of the order of 10° and in the downward bending direction of the finger is generally of the order of 90°, both measured with respect to the extended state illustrated in Figure 6.
  • the natural freedom of movement of the PIP is generally about 10° in the upward, over-extended direction and approximately 120° in the downward pinching direction.
  • the natural freedom of movement of the DIP joint measured with respect to the extended state illustrated in Figure 6, is generally approximately 10° in the upward, or over-extended direction, and is generally approximately 90° in the downward, bending or pinching direction.
  • the joint prosthesis has a considerable freedom of rotation in the said direction, for example a freedom of rotation of approximately 15°, i.e. up to a total of 25° with respect to the extended position. This has the advantage that stabilization against upward over-extending is supplied by the natural, or possibly completely or partially artificial, ligaments, so that these will continue to be exercised and will not weaken.

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  • Prostheses (AREA)

Abstract

The invention relates to a joint prosthesis comprising a first part (1) with a cylindrical socket (6) and a second part (2) with a cylindrical head (8). The cylindrical head (8) and socket (6) are of complementary form, in such a manner that together they are able to form a linear hinge. The cylindrical socket (6) extends over at most 180° in the circumferential direction. The cylindrical head (8) is provided with a radial thickened section (9) which extends in the circumferential direction. The cylindrical socket (6) is provided with a radial recess (7) which extends in the circumferential direction and in which the radial thickened section (9) can be accommodated, with the cylindrical head (8) in bearing contact inside the cylindrical socket (6). The radial thickened section (9) and radial recess (7) are arranged centrally and are formed so as to be self-aligning with respect to one another. The cylindrical head (8) may be arranged on at least one support arm (10) and one or both longitudinal edges (21) of the cylindrical socket (6) may be provided, in the area of the at least one support arm (10), with a cutout (17) in which the support arm (10) can be completely or partially accommodated.

Description

Joint prosthesis, in particular finger joint prosthesis
The present invention relates to a joint prosthesis comprising a first part with a cylindrical socket and a second part with a cylindrical head, the cylindrical head and socket being complementary to one another, in such a manner that together they are able to form a linear hinge which extends in the longitudinal direction of the head/socket. A prosthesis of this nature is known, in the form of a finger joint prosthesis, from US-A-3, 991, 425. A prosthesis of this nature, or at least a prosthesis which appears extremely similar, is also known under the name Djoa prosthesis. The Djoa prosthesis comprises a cylindrical roll surface in which a slot is formed. A hollow cylindrical socket runs over the cylindrical roll surface, with a projection which projects out of the socket fitting into the slot. The purpose of this projection is to prevent the socket from moving sideways, i.e. in the longitudinal direction of the linear hinge, with respect to the cylindrical roll surface, in order to ensure stability of the joint prosthesis in relation to loads which act in the longitudinal direction of the hinge. However, a drawback of this design is that in the event of such loads a force is exerted on the underlying bones to which the joint is attached, via the slot with the projection situated therein. As a result, the stems may be dislodged from the underlying bone or may break off, which would lead to considerable damage to the underlying bone.
GB patent specification 1,530,301 has disclosed a finger prosthesis which differs from the joint prosthesis according to the present invention in particular by the fact that the socket parts are fixed to the head parts by means of a snap-action connection, i.e. the socket parts extend over more than 180°, as is clear from the figures. Owing to the snap-action connection, this prosthesis, in the implanted position, does not allow any movement of the prosthesis parts with respect to one another apart from the pivoting movement about the longitudinal axis of the head parts/socket parts. It is not possible for the prosthesis parts to move apart from one another and to pivot with respect to one another transversely to the hinge direction.
DE-Offenlegungsschrift 2,814,752 has disclosed a two-part joint prosthesis, in which the first part comprises a fork with a socket part inside. The second part is provided with a head part which can be fixed to the socket part by means of a snap-action connection. Since the head part is of spherical or convex design, and the socket part is shaped accordingly, this joint prosthesis has two degrees of freedom. In addition to the main hinged movement, limited pivoting with respect to the main hinged movement is also possible. The prosthesis disclosed by DE-2,814,752 cannot move apart in the implanted position. The object of the present invention is to provide a joint prosthesis which, on the one hand, provides so-called medial/lateral stability, so that it is impossible for the moving parts to move in the longitudinal direction of the hinge with respect to one another, and, on the other hand, allows transverse forces, acting in the longitudinal direction of the hinge, on the bones which are connected by the joint without this inevitably leading to excessive load on the connection between the joint parts and the respective bones to which they are attached.
According to the invention, this object is achieved by means of a special design of the joint prosthesis, and in particular by the fact that: the cylindrical socket extends over at most 180° in the circumferential direction, the cylindrical head is provided with a radial thickened section which extends in the circumferential direction, and the cylindrical socket is provided with a radial recess which extends in the circumferential direction and in which the radial thickened section can be accommodated, preferably with the cylindrical head bearing inside the cylindrical socket .
In this design, since the cylindrical socket extends over at most 180°, the cylindrical head can be removed from the cylindrical socket by pulling it out in a direction which is parallel to or lies between the tangents at the free ends of the extent of the cylindrical socket. When the bone to which the cylindrical socket is attached extends in this direction, this essentially means that this bone is pulled away from the joint in its longitudinal direction. However, this also means that when, in this position, a transverse force which is directed in the longitudinal direction of the linear hinge acts on the said bone, this bone can undergo a pivoting movement, during which the cylindrical head comes out of the socket at one end of the linear hinge and is pressed against the socket at the other end of the linear hinge. Consequently, the action of such a transverse force on the connection between the prosthesis parts with the respective bones is reduced considerably. These transverse forces can then be absorbed entirely by the natural, or possibly artificial, ligaments which hold the joint together. If the cylindrical socket extends over less than 180°, the area in which such a tilting movement of the bone which is attached to the cylindrical socket with respect to the linear hinge can take place will be increased in size, as will be clear. However, an important advantage of the joint prosthesis according to the invention is that this so-called tilting freedom which has been outlined above decreases as the bone which is attached to the cylindrical head is situated further and further outside the area defined by the tangents at the free ends of the cylindrical head. Depending on the exact orientation of the cylindrical socket with respect to the underlying bone to which this socket is attached, a moment with respect to the longitudinal axis of the said bone will act on the said bone. Such a rotation can then be absorbed, in the case where there is a joint at the other end of the said bone, by the said joint or by the ligaments associated with the said joint. Generally, the cylindrical socket will be oriented in such a manner, with respect to the bone to which it is attached, that the cylindrical head can be removed from this socket when the two bones are situated essentially in line with one another. As will be clear to a person skilled in the art, such a joint prosthesis according to the invention can generally be used with very great success for finger joint prostheses, toe joint prostheses, and possibly elbow or knee prostheses.
In order to achieve a so-called pivoting freedom or tilting freedom of the joint prosthesis which is equal in both opposite directions (also known in the specialist medical field as the medial and lateral directions) , it is advantageous, according to the invention, if the radial thickened section and the radial recess are arranged centrally, as seen in the longitudinal direction of the linear hinge. In order to ensure that after a so-called tilting or pivoting of the joint parts with respect to one another, the cylindrical head moves correctly back into the cylindrical socket (i.e. with their cylinder axes essentially coinciding) , it is advantageous, according to the invention, if the radial thickened section and/or the radial recess are formed so as to be self-aligning with respect to one another. It will be clear to a person skilled in the art that a self- aligning effect of this nature can be achieved in a wide variety of ways by suitable shaping of circumferential sides, which extend in particular in the circumferential direction, of the radial thickened section and/or the radial recess. According to the invention, the self-aligning effect can be achieved, inter alia, by providing the circumferential sides of the radial thickened section with bevels and/or rounded portions, optionally in combination with bevels and/or rounded portions on the circumferential sides of the radial recess.
In order, on the one hand, to provide sufficient medial/lateral stability, i.e. resistance to displacement of the joint-prosthesis parts with respect to one another in the longitudinal direction of the linear hinge and, on the other hand, to allow the radial thickened section and the radial recess to be self-aligning with respect to one another, it is advantageous, according to the invention, if the circumferential sides, which extend in the circumferential direction, of the radial thickened section and/or of the radial recess comprise an active circumferential side face which includes an angle of approximately 1° to approximately 10° with a radially oriented transverse plane. These side faces therefore do not extend at right angles to the axis of rotation of the linear hinge, but rather at a relatively small angle with respect to a radial transverse plane which is perpendicular to the said hinge axis.
In order to be able to increase the maximum freedom of rotation of the joint prosthesis with respect to the maximum freedom of rotation permitted by the extent of the cylindrical head itself (also known in the medical field as the flexural freedom) , it is advantageous according to the invention, in the case where the cylindrical head is arranged on the end of at least one support arm which extends radially with respect to the cylindrical head, if one or both longitudinal edge(s) of the cylindrical socket are provided, in the area of the at least one support arm, with a cutout in which the cross section of the support arm can be completely or partially accommodated.
In order to prevent the functioning or effectiveness of the natural ligaments which hold the joint (in this case the joint prosthesis) together from decreasing, it is advantageous, according to the invention, if the freedom of rotation of the linear hinge in one or both direction (s) of rotation is greater than the associated freedom of rotation (medical: flexural freedom) of the natural joint which the joint prosthesis is intended to replace. This ensures that the freedom of rotation is limited not by the joint prosthesis but by the original, natural or possibly completely or partly artificial ligaments. The extent to which this freedom of rotation of the joint prosthesis is greater than that of the natural joint will preferably be approximately 5° to approximately 20°, such as for example, and more preferably, approximately 15°. In order in particular to design the joint prosthesis to be extremely small while nevertheless able to withstand high loads, it is advantageous, according to the invention, if the first part and the second part are each a metal part, for example are each a single-piece metal part. It is thus possible to produce joint prostheses which, in relative terms, are extremely small and yet strong, such as for example finger joint prostheses. The metal parts are in this case preferably made from a chromium-cobalt alloy, as is known per se from the prior art for prostheses and joint prostheses.
In order to improve the friction properties at the contact surfaces of the joint-prosthesis parts which can move with respect to one another, it is advantageous, according to the invention, if the first part and the second part, or at least the contact surfaces of the cylindrical head and cylindrical socket, are coated with a suitable coating material.
In order to counteract rejection and other undesirable interactions between the joint prosthesis and the surrounding human or animal tissue, it is advantageous, according to the invention, if the first and second parts, or at least their external surfaces, are made from or coated with a material which is compatible with the human, or if appropriate animal, body, i.e. in particular a material which is compatible with the human, or if appropriate animal, body without entering into chemical reactions therewith, or at least without entering into any adverse and/or undesirable chemical reactions therewith.
Since in many joints a so-called tilting or pivoting freedom is desirable or required only within a limited rotational position of the adjoining bones with respect to one another, it is advantageous, according to the invention, if the cylindrical socket extends over at least 160°, preferably over at least 170°, in the circumferential direction.
The joint prosthesis according to the invention can be used in particular as a finger joint prosthesis, such as an MCP prosthesis ( CP = metacarpophalangeal) or in particular a PIP prosthesis (PIP = proximal interphalangeal) . Although prostheses are used relatively infrequently at the DIP joint (DIP = distal interphalangeal) , since they are deemed less useful, it should be noted that the joint prosthesis according to the invention can also be used with considerable success as a DIP prosthesis. The same comments as those made in relation to the DIP prosthesis should also be noted in relation to toe joint prostheses, for which the joint prosthesis according to the invention can also be used with considerable success.
Depending on the specific location where the joint prosthesis according to the invention is used, it will be possible to adapt the orientation of the cylindrical socket with respect to the bone which is to be connected thereto, as well as the extent in the circumferential direction of the cylindrical socket, as well as the one or more cutouts for accommodating the support arm, in order to increase the freedom of rotation of the joint prosthesis in relation to the freedom of rotation permitted by the cylindrical socket . In the following text, the present invention will be explained in more detail with reference to examples illustrated in the drawings, in which:
Figure 1 shows a perspective view of a joint prosthesis according to the invention in the so-called extended state;
Figure 2 shows a perspective view of the embodiment shown in Figure 1, but with the parts of the joint prosthesis taken apart; Figure 3 shows a side view, partially in section, of a joint prosthesis in accordance with the embodiment shown in Figures 1 and 2 which has been pivoted into a limit position;
Figure 4 shows a rear view, from the direction of arrow IV, of one part of the joint prosthesis according to the invention;
Figure 5 shows an extremely diagrammatic sketch of the cylindrical socket, on the basis of which the directions in which the cylindrical head can be removed from the cylindrical socket are indicated; and
Figure 6 shows a diagrammatic view of the bones and joints of which a finger is composed.
Figure 1 shows a diagrammatic, perspective view of a so-called PIP prosthesis, the view being from above onto the underside, in the implanted position, of the joint prosthesis, i.e. the side which lies on the inside of the hand in the implanted position. In this case, joint part 1 is the proximal joint part, which lies on the carpal (metacarpal) side of the joint, i.e. that side of the joint which is directed towards the hand. The joint part 2 is the distal joint part which lies on that side of the joint which is directed towards the fingertips. Both joint parts comprise a stem which is known per se, or at least is nothing special, and by means of which the joint prosthesis can be attached in a respective phalangeal bone of the hand using techniques which are known per se. It is entirely within the scope of the invention for these stems 3 and 4 also to be of different design, for example as a multiple stem for mutually parallel pins or with a different shape from that which is illustrated in the figures .
The proximal part 1 is provided with a head 5, in which a cylindrical socket 6 is formed. The centre of the cylindrical socket 6 is provided with a recess 7 which extends in the circumferential direction of the cylindrical socket 6, divides the cylindrical socket 6 in two and is likewise of cylindrical form. This recess 7 thus forms, as it were, a deeper, additional cylindrical socket surface between the two parts of the cylindrical socket 6. The cylindrical socket 6, or at least its purely central part, extends over 175 to 180°, and will preferably extend over approximately 180°.
The distal part 2 of the joint prosthesis is provided with a cylindrical head 8 which extends essentially over 360° and is provided in its centre with a radial thickened section 9 which extends over virtually the entire circumference of the cylindrical head 8. Those parts of the cylindrical head 8 which lie next to the central thickened section extend over 360°. The radial thickened section 9 extends over less than 360°, since it is interrupted by a support arm 10, via which the cylindrical head 8, 9 is connected to the stem 4. An oval flange 11 is formed between the support arm 10 and the stem 4, providing support on the underlying bone and preventing the distal part 2 of the joint prosthesis from being pressed too deep into the associated bone.
The cylindrical head 8 and cylindrical socket 6 are shaped so as to complement one another, in such a manner that the cylindrical head 8 can be accommodated in the cylindrical socket 6 and can execute a hinged movement about the common, describing cylinder axis. In this case, the width of the thickened section 9, as seen in the direction of the hinge axis 12, i.e. in the longitudinal direction of the head/socket, is essentially equal to the width of the recess 7 in the cylindrical socket 6, as seen in the same direction. Furthermore, the thickened section 9 is dimensioned in such a manner that it can be accommodated entirely inside the recess 7, in which position there is no need for the cylindrical circumferential surfaces, which run parallel to the longitudinal direction, of the recess and the thickened section as such to be in contact with one another. It will be clear that the thickened section 9 thus prevents the distal joint prosthesis part 2 from being displaced in the longitudinal direction of the linear hinge with respect to the proximal joint prosthesis part 1, since the essentially radial circumferential side faces 14 of the thickened section 9 and the essentially radial circumferential side faces 13 of the recess will be in contact, or virtually in contact, with one another.
The distal joint prosthesis part 2 may execute a pivoting movement, in the direction of arrow 15, with respect to the proximal joint prosthesis part 1, in which case one end of the cylindrical head 8 will come out of the cylindrical socket 6 and the other, opposite end of the cylindrical head 8 will be pressed into the cylindrical socket 6. In this way, a force which acts on the distal phalangeal bone of the hand in the transverse direction, indicated by arrow F, can result in tilting or pivoting, in the direction of arrow 15, of the distal joint prosthesis part 2 with respect to the proximal joint prosthesis part 1, without this leading to a load being imposed on the connection between the stems 3 and 4 and the proximal phalangeal bone of the hand or distal bone of the hand, since the pivoting indicated by arrow 15 and caused by the transverse force F is then absorbed by the natural or artificial joint ligaments. In order, after such pivoting of the distal joint prosthesis part 2 with respect to the proximal joint prosthesis part 1 in the direction of arrow 15, to ensure that the cylindrical head moves correctly into the cylindrical socket, in particular the thickened section moves correctly into the recess, under the influence of the restoring force exerted by the joint ligaments, the thickened section and/or recess are preferably both shaped so as to be self- aligning. According to the invention, this can be achieved, inter alia, by bevelling the circumferential sides 14 of the thickened section 9 at 15 and by bevelling the circumferential sides 13 of the recess 7 at 16. According to the invention, the self-aligning action can be improved further by providing the circumferential sides 14 circumferential side faces which slope slightly towards one another in the radially outward direction, for example each slope at an angle of from 1 to 10° with respect to a transverse plane which is perpendicular to the hinge axis 12. In a corresponding way, the circumferential sides of the recess can be provided with circumferential sides faces which slope towards one another in the same direction, also preferably at an angle of from 1 to 10° with respect to a transverse plane which is perpendicular to the hinge axis 12.
As can be seen from Figures 1, 2 and 3, the cylindrical socket 6 is provided with a cutout 17 on its underside, which is shown as the top side in Figures 1 and as the underside in Figure 3. The dimensions of the cutout 17 are such that it is able to accommodate the support arm 10, so that the freedom of rotation of the distal joint prosthesis part 2 with respect to that of the proximal joint prosthesis part 1 is made greater than the extent in the circumferential direction of the cylindrical socket would inherently allow. In this way, it is possible for the distal joint prosthesis part 2 to be over-extended, by an angle α of 25°, in the upwards direction with respect to the extended position illustrated in Figure 3 by the axis 18 (in the medical field, this is also known by the term hyperextension) , and also that the distal joint prosthesis part 2 can rotate downwards, in the anticlockwise direction, over an angle β of 125° in the downwards direction (also known in the medical field by the term flection) .
Figure 5 provides a very diagrammatic side view of a cylindrical socket which extends over 150° in the circumferential direction. 61 and 62 are in this case the tangents on the opposite ends of the cylindrical extent of the socket 60. These tangents 61 and 62, with their intersection point, together determine a range γ of tension directions T via which the cylindrical head can be pulled out of the cylindrical socket. The arrow T in this case runs within the tangent lines 61 and 62 and intersects the intersection of these tangents.
Figure 6 provides a highly diagrammatic illustration of the bones of a finger and the joints of a finger. 71 denotes the carpal bones, which for their part comprise a number of small bones and joints, 72 denotes the proximal phalange, 73 denotes the middle phalange and 74 denotes the distal phalange. The joint 75, as indicated by the letters MCP, is the so-called metacarpophalangeal joint, 76 is the so-called PIP (proximal interphalangeal) joint, and 77 is the so- called DIP (distal interphalangeal) joint. The natural freedom of movement of an MCP is, in the upward overextended direction, generally of the order of 10° and in the downward bending direction of the finger is generally of the order of 90°, both measured with respect to the extended state illustrated in Figure 6.
The natural freedom of movement of the PIP, again measured with respect to the extended state illustrated in Figure 6, is generally about 10° in the upward, over-extended direction and approximately 120° in the downward pinching direction.
The natural freedom of movement of the DIP joint, measured with respect to the extended state illustrated in Figure 6, is generally approximately 10° in the upward, or over-extended direction, and is generally approximately 90° in the downward, bending or pinching direction. In particular, with regard to the upward over- extending direction, it is advantageous according to the invention if the joint prosthesis has a considerable freedom of rotation in the said direction, for example a freedom of rotation of approximately 15°, i.e. up to a total of 25° with respect to the extended position. This has the advantage that stabilization against upward over-extending is supplied by the natural, or possibly completely or partially artificial, ligaments, so that these will continue to be exercised and will not weaken. Such additional freedom of rotation of the joint prosthesis may also be useful with regard to the downward pinching or gripping movement . As will be clear from Figure 3, in the hinged state indicated by solid lines, pivoting of the distal joint prosthesis part 2 in a plane perpendicular to the plane of the drawing in accordance with Figure 3 will be impeded by the top side 19 of the cylindrical socket 6. Instead of such a mutual tilting or pivoting movement, a moment will then be exerted on the proximal joint prosthesis part 1, which moment seeks to rotate the joint prosthesis part 1 about its longitudinal axis 20. In the case of a PIP joint prosthesis, this rotational moment about axis 20 will then be absorbed by the ligaments of the MCP joint.

Claims

Claims
1. Joint prosthesis comprising a first part (1) with a cylindrical socket (6) and a second part (2) with a cylindrical head (8), the cylindrical head (8) and socket (6) being complementary to one another, in such a manner that together they are able to form a linear hinge which extends in the longitudinal direction (12) of the head/socket (6/8), characterized - in that the cylindrical socket (6) extends over at most 180┬░ in the circumferential direction, in that the cylindrical head (8) is provided with a radial thickened section (9) which extends in the circumferential direction, and - in that the cylindrical socket (6) is provided with a radial recess (7) which extends in the circumferential direction and in which the radial thickened section (9) can be accommodated, preferably with the cylindrical head (6) being in bearing contact inside the cylindrical socket (8).
2. Joint prosthesis according to Claim 1, characterized in that the tangent extent of the lines at the free ends of the cylindrical socket define a range of removal directions for removing the head from the socket, the longitudinal direction of a bone to which the cylindrical head is to be attached or of a stem (3) which is to be attached inside a bone and bears the socket (6) at one end lying within the said range of removal directions.
3. Joint prosthesis according to Claim 1 or 2, in which the first part (1) and the second part (2) each comprise a respective stem (3 or 4, respectively), which at one free end respectively bears the cylindrical socket or the cylindrical head, and which can each be attached in a respective bone part, characterized in that the cylindrical socket is oriented in such a way with respect to the stem (3) of the first part (1) that the cylindrical head (8) can be taken out of the cylindrical socket (6) when the two stems are essentially aligned with one another.
4. Joint prosthesis according to one of the preceding claims, characterized in that the radial thickened section (9) and radial recess (7) are arranged centrally, as seen in the longitudinal direction (12) .
5. Joint prosthesis according to one of the preceding claims, characterized in that the radial thickened section (9) and/or the radial recess (7) are formed so as to be self-aligning with respect to one another .
6. Joint prosthesis according to Claim 5, characterized in that the circumferential sides (14), which extend in the circumferential direction, of the radial thickened section (9) are provided with bevels and/or rounded portions (16).
7. Joint prosthesis according to Claim 5 or 6, characterized in that the circumferential sides (13), which extend in the circumferential direction, of the radial recess (7) are provided with bevels and/or rounded portions (16) .
8. Joint prosthesis according to one of the preceding claims, characterized in that the circumferential sides, which extend in the circumferential direction, of the radial thickened section (9) and/or of the radial recess (7) comprise an active circumferential side face (14 or 13, respectively) which includes an angle of approximately 1┬░ to 10┬░ with a radially oriented transverse plane.
9. Joint prosthesis according to one of the preceding claims, characterized in that the cylindrical head (8) is arranged on the end of at least one support arm (10) which extends radially with respect to the cylindrical head (8), and in that one or both longitudinal edge(s) (21) of the cylindrical socket (6) is/are provided, in the area of the at least one support arm (10), with a cutout (13) in which the cross section of the support arm (10) can be completely or partially accommodated.
10. Joint prosthesis according to one of the preceding claims, characterized in that the freedom of rotation of the linear hinge in one or both direction (s) of rotation is greater than the associated freedom of rotation of the natural joint which the joint prosthesis is intended to replace.
11. Joint prosthesis according to Claim 10, characterized in that the extent to which the said freedom of rotation of the joint prosthesis is greater than that of the natural joint is approximately 5┬░ to approximately 20┬░, for example approximately 15┬░.
12. Joint prosthesis according to one of the preceding claims, characterized in that the first part
(1) and second part (2) are each a metal part, for example are each a single-piece metal part.
13. Joint prosthesis according to Claim 12, characterized in that the metal parts are made from a chromium-cobalt alloy.
14. Joint prosthesis according to one of the preceding claims, characterized in that the first part
(1) and second part (2) , or at least the contact surfaces of the cylindrical head (8) and cylindrical socket (6), are coated with a coating material.
15. Joint prosthesis according to one of the preceding claims, characterized in that the first part
(1) and second part (2), or at least their external surfaces, are made from or coated with a material which is compatible with the human body.
16. Joint prosthesis according to one of the preceding claims, characterized in that the cylindrical socket (6) extends over at least 160┬░, preferably over at least 170┬░, more preferably over approximately 180┬░ in the circumferential direction.
17. Joint prosthesis according to one of the preceding claims, characterized in that it is a finger joint prosthesis, such as an MCP prosthesis or in particular a PIP prosthesis.
18. Use of a joint prosthesis according to one of Claims 1 to 16 as a finger prosthesis, such as an MCP prosthesis or in particular a PIP prosthesis.
PCT/NL1999/000413 1998-07-03 1999-07-02 Joint prosthesis, in particular finger joint prosthesis WO2000001327A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP99931585A EP1094766B1 (en) 1998-07-03 1999-07-02 Joint prosthesis, in particular finger joint prosthesis
AT99931585T ATE262862T1 (en) 1998-07-03 1999-07-02 JOINT PROSTHESIS, IN PARTICULAR FINGER JOINT PROSTHESIS
JP2000557775A JP2004525652A (en) 1998-07-03 1999-07-02 Artificial joints, especially finger joints
AU48036/99A AU4803699A (en) 1998-07-03 1999-07-02 Joint prosthesis, in particular finger joint prosthesis
US09/720,983 US6352560B1 (en) 1998-07-03 1999-07-02 Joint prosthesis
DE69916064T DE69916064T2 (en) 1998-07-03 1999-07-02 JOINT PROSTHESIS, IN PARTICULAR FINGER JOINT PROSTHESIS

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL1009550 1998-07-03
NL1009550A NL1009550C2 (en) 1998-07-03 1998-07-03 Joint prosthesis, in particular finger joint prosthesis.

Publications (2)

Publication Number Publication Date
WO2000001327A2 true WO2000001327A2 (en) 2000-01-13
WO2000001327A3 WO2000001327A3 (en) 2000-02-24

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PCT/NL1999/000413 WO2000001327A2 (en) 1998-07-03 1999-07-02 Joint prosthesis, in particular finger joint prosthesis

Country Status (8)

Country Link
US (1) US6352560B1 (en)
EP (1) EP1094766B1 (en)
JP (1) JP2004525652A (en)
AT (1) ATE262862T1 (en)
AU (1) AU4803699A (en)
DE (1) DE69916064T2 (en)
NL (1) NL1009550C2 (en)
WO (1) WO2000001327A2 (en)

Cited By (6)

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Publication number Priority date Publication date Assignee Title
WO2002039933A1 (en) * 2000-11-16 2002-05-23 Willi Horber Endoprosthesis for a shoulder joint
FR2843016A1 (en) * 2002-07-31 2004-02-06 Jean Claude Bouvet Articulating digit prosthesis for restoring articulation between two phalanges, e.g. between metacarpal bone and proximal phalange e.g. due to rheumatoid arthritis, includes pivot housed in reception chamber
US6749637B1 (en) 1999-09-24 2004-06-15 Baehler Andre Endoprosthesis for a shoulder joint
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DE69916064D1 (en) 2004-05-06
NL1009550C2 (en) 2000-01-10
WO2000001327A3 (en) 2000-02-24
EP1094766B1 (en) 2004-03-31
JP2004525652A (en) 2004-08-26
ATE262862T1 (en) 2004-04-15
EP1094766A2 (en) 2001-05-02
AU4803699A (en) 2000-01-24
DE69916064T2 (en) 2004-08-05
US6352560B1 (en) 2002-03-05

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